Canonical Allele Identifier: CA2420210082
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015528G= , CM000685.2:g.25015528G= GRCh38
NC_000023.10:g.25033645G= , CM000685.1:g.25033645G= GRCh37
NC_000023.9:g.24943566G= NCBI36
NG_008281.1:g.5421C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.196+14C= MANE Select ENSP00000368332.4:n.196+14C=
ENST00000379044.4:c.196+14C= ENSP00000368332.4:n.196+14C=
NM_139058.2:c.196+14C= NP_620689.1:n.196+14C=
NM_139058.3:c.196+14C= MANE Select NP_620689.1:n.196+14C=